![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: SCD5 |
Gene summary for SCD5 |
![]() |
Gene information | Species | Human | Gene symbol | SCD5 | Gene ID | 79966 |
Gene name | stearoyl-CoA desaturase 5 | |
Gene Alias | ACOD4 | |
Cytomap | 4q21.22 | |
Gene Type | protein-coding | GO ID | GO:0006082 | UniProtAcc | Q86SK9 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
79966 | SCD5 | CCI_1 | Human | Cervix | CC | 3.15e-05 | 7.78e-01 | 0.528 |
79966 | SCD5 | CCI_2 | Human | Cervix | CC | 2.62e-08 | 9.30e-01 | 0.5249 |
79966 | SCD5 | CCI_3 | Human | Cervix | CC | 1.82e-05 | 4.77e-01 | 0.516 |
79966 | SCD5 | LZE7T | Human | Esophagus | ESCC | 2.63e-05 | 1.15e-01 | 0.0667 |
79966 | SCD5 | LZE8T | Human | Esophagus | ESCC | 3.77e-04 | 1.42e-01 | 0.067 |
79966 | SCD5 | LZE24T | Human | Esophagus | ESCC | 3.84e-10 | 1.98e-01 | 0.0596 |
79966 | SCD5 | P1T-E | Human | Esophagus | ESCC | 9.79e-03 | 6.49e-02 | 0.0875 |
79966 | SCD5 | P2T-E | Human | Esophagus | ESCC | 3.74e-27 | 6.12e-01 | 0.1177 |
79966 | SCD5 | P4T-E | Human | Esophagus | ESCC | 7.08e-20 | 2.41e-01 | 0.1323 |
79966 | SCD5 | P5T-E | Human | Esophagus | ESCC | 1.94e-06 | 2.97e-02 | 0.1327 |
79966 | SCD5 | P8T-E | Human | Esophagus | ESCC | 3.46e-17 | 4.36e-01 | 0.0889 |
79966 | SCD5 | P9T-E | Human | Esophagus | ESCC | 1.89e-12 | 1.60e-01 | 0.1131 |
79966 | SCD5 | P10T-E | Human | Esophagus | ESCC | 2.63e-39 | 7.32e-01 | 0.116 |
79966 | SCD5 | P11T-E | Human | Esophagus | ESCC | 1.36e-11 | 5.61e-01 | 0.1426 |
79966 | SCD5 | P12T-E | Human | Esophagus | ESCC | 4.16e-23 | 5.83e-01 | 0.1122 |
79966 | SCD5 | P15T-E | Human | Esophagus | ESCC | 1.44e-24 | 4.94e-01 | 0.1149 |
79966 | SCD5 | P16T-E | Human | Esophagus | ESCC | 1.97e-12 | 2.60e-01 | 0.1153 |
79966 | SCD5 | P17T-E | Human | Esophagus | ESCC | 4.80e-06 | 3.35e-01 | 0.1278 |
79966 | SCD5 | P20T-E | Human | Esophagus | ESCC | 2.22e-10 | 1.58e-01 | 0.1124 |
79966 | SCD5 | P21T-E | Human | Esophagus | ESCC | 4.75e-17 | 1.76e-01 | 0.1617 |
Page: 1 2 3 4 5 |
![]() |
∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
Top |
Malignant transformation related pathway analysis |
![]() |
![]() |
Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | CRC | ![]() |
Stomach | GC | ![]() |
Stomach | CAG with IM | ![]() |
Stomach | CSG | ![]() |
Stomach | CAG | ![]() |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
Page: 1 2 3 4 5 6 7 8 9 |
![]() |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00066318 | Esophagus | ESCC | fatty acid metabolic process | 217/8552 | 390/18723 | 4.21e-05 | 3.39e-04 | 217 |
GO:00463948 | Esophagus | ESCC | carboxylic acid biosynthetic process | 175/8552 | 314/18723 | 1.98e-04 | 1.26e-03 | 175 |
GO:00160538 | Esophagus | ESCC | organic acid biosynthetic process | 175/8552 | 316/18723 | 3.04e-04 | 1.82e-03 | 175 |
GO:00160537 | Oral cavity | OSCC | organic acid biosynthetic process | 155/7305 | 316/18723 | 1.64e-04 | 1.13e-03 | 155 |
GO:00463947 | Oral cavity | OSCC | carboxylic acid biosynthetic process | 154/7305 | 314/18723 | 1.73e-04 | 1.19e-03 | 154 |
GO:00066317 | Oral cavity | OSCC | fatty acid metabolic process | 186/7305 | 390/18723 | 2.65e-04 | 1.69e-03 | 186 |
GO:00066363 | Oral cavity | OSCC | unsaturated fatty acid biosynthetic process | 28/7305 | 51/18723 | 1.54e-02 | 4.99e-02 | 28 |
Page: 1 |
![]() |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0415210 | Esophagus | ESCC | AMPK signaling pathway | 80/4205 | 121/8465 | 1.73e-04 | 6.67e-04 | 3.42e-04 | 80 |
hsa012129 | Esophagus | ESCC | Fatty acid metabolism | 41/4205 | 57/8465 | 5.13e-04 | 1.75e-03 | 8.98e-04 | 41 |
hsa0415213 | Esophagus | ESCC | AMPK signaling pathway | 80/4205 | 121/8465 | 1.73e-04 | 6.67e-04 | 3.42e-04 | 80 |
hsa0121214 | Esophagus | ESCC | Fatty acid metabolism | 41/4205 | 57/8465 | 5.13e-04 | 1.75e-03 | 8.98e-04 | 41 |
hsa041529 | Oral cavity | OSCC | AMPK signaling pathway | 71/3704 | 121/8465 | 6.29e-04 | 1.86e-03 | 9.49e-04 | 71 |
hsa049365 | Oral cavity | OSCC | Alcoholic liver disease | 78/3704 | 142/8465 | 4.53e-03 | 1.12e-02 | 5.68e-03 | 78 |
hsa012128 | Oral cavity | OSCC | Fatty acid metabolism | 35/3704 | 57/8465 | 5.37e-03 | 1.29e-02 | 6.55e-03 | 35 |
hsa0415212 | Oral cavity | OSCC | AMPK signaling pathway | 71/3704 | 121/8465 | 6.29e-04 | 1.86e-03 | 9.49e-04 | 71 |
hsa0493612 | Oral cavity | OSCC | Alcoholic liver disease | 78/3704 | 142/8465 | 4.53e-03 | 1.12e-02 | 5.68e-03 | 78 |
hsa0121213 | Oral cavity | OSCC | Fatty acid metabolism | 35/3704 | 57/8465 | 5.37e-03 | 1.29e-02 | 6.55e-03 | 35 |
Page: 1 |
Top |
Cell-cell communication analysis |
![]() |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
![]() |
TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
Page: 1 |
Top |
Somatic mutation of malignant transformation related genes |
![]() |
Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
SCD5 | SNV | Missense_Mutation | c.88N>T | p.Gly30Cys | p.G30C | Q86SK9 | protein_coding | tolerated(0.06) | benign(0.374) | TCGA-A1-A0SK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |
SCD5 | SNV | Missense_Mutation | rs369204191 | c.223N>G | p.Leu75Val | p.L75V | Q86SK9 | protein_coding | tolerated(0.37) | benign(0.1) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
SCD5 | SNV | Missense_Mutation | rs781504369 | c.484C>T | p.Arg162Cys | p.R162C | Q86SK9 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
SCD5 | SNV | Missense_Mutation | rs868598058 | c.265N>A | p.Val89Met | p.V89M | Q86SK9 | protein_coding | deleterious(0) | probably_damaging(0.977) | TCGA-AN-A0AK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
SCD5 | SNV | Missense_Mutation | rs200922750 | c.445N>T | p.Arg149Trp | p.R149W | Q86SK9 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AA-3696-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
SCD5 | SNV | Missense_Mutation | rs770103071 | c.742C>T | p.Arg248Trp | p.R248W | Q86SK9 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-AA-3710-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
SCD5 | SNV | Missense_Mutation | c.289N>C | p.Trp97Arg | p.W97R | Q86SK9 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-G4-6586-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
SCD5 | SNV | Missense_Mutation | c.884N>G | p.Thr295Ser | p.T295S | Q86SK9 | protein_coding | deleterious(0.03) | benign(0.411) | TCGA-RU-A8FL-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD | |
SCD5 | SNV | Missense_Mutation | rs762891080 | c.557N>A | p.Arg186Gln | p.R186Q | Q86SK9 | protein_coding | tolerated(0.15) | benign(0.025) | TCGA-AF-6136-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | 5-fluorouracil | PD |
SCD5 | SNV | Missense_Mutation | rs770103071 | c.742C>T | p.Arg248Trp | p.R248W | Q86SK9 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-AJ-A3BG-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Chemotherapy | carboplatin | PD |
Page: 1 2 3 4 |
Top |
Related drugs of malignant transformation related genes |
![]() |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |